COMPLIANCE ADVISORY
EU In Vitro Diagnostic Medical Devices Regulation (IVDR) Readiness Advisory
A strategy call with someone who has spent 25 years building compliance systems used by 100,000+ professionals in 160+ countries – not a generalist who read the standard last week.
Why work with Ivanka on EU In Vitro Diagnostic Medical Devices Regulation (IVDR)
The EU In Vitro Diagnostic Regulation (EU 2017/746) establishes the regulatory framework for IVD medical devices in the European Union. Effective May 26, 2022 (with transitional provisions through 2028), it replaces the IVD Directive 98/79/EC. IVDR introduces a new risk-based classification system (Class A-D), strengthened conformity assessment, and enhanced post-market surveillance requirements.
Most consultants approach EU In Vitro Diagnostic Medical Devices Regulation (IVDR) as a checkbox exercise. Ivanka approaches it as a strategic lever. With 25 years of building The Art of Service – a compliance platform now covering 692 frameworks and 819,000+ cross-framework mappings – she doesn't just understand the standard. She understands how it connects to everything else your organisation is already doing.
This matters because EU In Vitro Diagnostic Medical Devices Regulation (IVDR) doesn't exist in isolation. Ivanka will map your current compliance posture against the 23 controls across 6 domains, identify gaps, and show you where existing controls from other frameworks you may already follow can be leveraged – saving months of redundant work.
Relevant credentials
- Experience guiding healthcare organisations through complex regulatory compliance landscapes
- MIT Entrepreneurial Masters graduate – rigorous analytical approach to enterprise challenges
- EXIN Expert Panel member – helping shape global certification standards
THE STRATEGY CALL
What you get in 30 minutes
Ivanka reviews your EU In Vitro Diagnostic Medical Devices Regulation (IVDR) readiness scores and identifies the critical gaps that carry the highest risk. No generic advice – specific to your domains and controls.
A clear, prioritised plan for addressing gaps across 6 domains. She maps what you can leverage from existing compliance work and what requires new investment.
EU In Vitro Diagnostic Medical Devices Regulation (IVDR) maps to 352 other frameworks. Ivanka shows you where a single control implementation can satisfy multiple regulatory requirements at once.
Domains covered in EU In Vitro Diagnostic Medical Devices Regulation (IVDR)
Plus 1 additional domains. See the full assessment →
This is for you if
- You need to achieve EU In Vitro Diagnostic Medical Devices Regulation (IVDR) compliance but don’t know where to start or how to prioritise
- You’ve been told you’re “compliant” but suspect gaps exist that haven’t been properly assessed
- You manage compliance for healthcare organisations and need expert guidance, not generic templates
- You want to leverage existing compliance efforts across multiple frameworks rather than starting from scratch
- You need a strategic plan your leadership team and board will actually understand and support
Start with a free assessment. Then let's talk strategy.
Take the free EU In Vitro Diagnostic Medical Devices Regulation (IVDR) readiness diagnostic. In 5 minutes you'll have a clear picture of where your gaps are. Then book the strategy call and Ivanka will show you exactly how to close them.
Free · No login required · Results in 5 minutes
Or go directly to the $149 Report + Strategy Call